Information on Organism Pochonia chlamydosporia

TaxTree of Organism Pochonia chlamydosporia
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PATHWAY
BRENDA Link
KEGG Link
MetaCyc Link
(S)-propane-1,2-diol degradation
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3-methylbutanol biosynthesis (engineered)
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acetaldehyde biosynthesis I
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acetylene degradation (anaerobic)
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alpha-Linolenic acid metabolism
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Biosynthesis of secondary metabolites
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butanol and isobutanol biosynthesis (engineered)
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chitin degradation to ethanol
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Chloroalkane and chloroalkene degradation
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Drug metabolism - cytochrome P450
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ethanol degradation I
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ethanol degradation II
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ethanol fermentation
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ethanolamine utilization
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Fatty acid degradation
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Glycine, serine and threonine metabolism
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Glycolysis / Gluconeogenesis
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heterolactic fermentation
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L-isoleucine degradation II
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L-leucine degradation III
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L-methionine degradation III
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L-phenylalanine degradation III
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L-tryptophan degradation V (side chain pathway)
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L-tyrosine degradation III
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L-valine degradation II
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leucine metabolism
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Metabolic pathways
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Metabolism of xenobiotics by cytochrome P450
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methionine metabolism
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Microbial metabolism in diverse environments
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mixed acid fermentation
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Naphthalene degradation
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noradrenaline and adrenaline degradation
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phenylalanine metabolism
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phenylethanol biosynthesis
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phytol degradation
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propanol degradation
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pyruvate fermentation to ethanol I
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pyruvate fermentation to ethanol II
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pyruvate fermentation to ethanol III
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pyruvate fermentation to isobutanol (engineered)
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Retinol metabolism
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salidroside biosynthesis
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serotonin degradation
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superpathway of fermentation (Chlamydomonas reinhardtii)
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Tyrosine metabolism
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tyrosine metabolism
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valine metabolism
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baicalein degradation (hydrogen peroxide detoxification)
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betanidin degradation
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justicidin B biosynthesis
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luteolin triglucuronide degradation
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matairesinol biosynthesis
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non-pathway related
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Phenylpropanoid biosynthesis
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sesamin biosynthesis
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nicotine degradation IV
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1,5-anhydrofructose degradation
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acetone degradation I (to methylglyoxal)
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acetone degradation III (to propane-1,2-diol)
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Amaryllidacea alkaloids biosynthesis
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Aminobenzoate degradation
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Arachidonic acid metabolism
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arachidonic acid metabolism
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bupropion degradation
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Caffeine metabolism
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Linoleic acid metabolism
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melatonin degradation I
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nicotine degradation V
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Steroid hormone biosynthesis
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Tryptophan metabolism
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vanillin biosynthesis I
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capsaicin biosynthesis
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chlorogenic acid biosynthesis I
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coumarins biosynthesis (engineered)
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Flavonoid biosynthesis
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phenylpropanoid biosynthesis
phenylpropanoids methylation (ice plant)
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scopoletin biosynthesis
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Stilbenoid, diarylheptanoid and gingerol biosynthesis
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suberin monomers biosynthesis
Biosynthesis of 12-, 14- and 16-membered macrolides
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erythromycin D biosynthesis
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Cyanoamino acid metabolism
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gamma-glutamyl cycle
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Glutathione metabolism
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glutathione metabolism
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hypoglycin biosynthesis
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leukotriene biosynthesis
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Taurine and hypotaurine metabolism
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Amino sugar and nucleotide sugar metabolism
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chitin biosynthesis
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4-hydroxy-2-nonenal detoxification
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camalexin biosynthesis
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Drug metabolism - other enzymes
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gliotoxin biosynthesis
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glutathione-mediated detoxification I
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glutathione-mediated detoxification II
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indole glucosinolate activation (intact plant cell)
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pentachlorophenol degradation
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Starch and sucrose metabolism
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chitin degradation I (archaea)
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chitin degradation II (Vibrio)
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chitin degradation III (Serratia)
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anhydromuropeptides recycling I
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anhydromuropeptides recycling II
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Glycosaminoglycan degradation
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Glycosphingolipid biosynthesis - ganglio series
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Glycosphingolipid biosynthesis - globo and isoglobo series
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Other glycan degradation
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Various types of N-glycan biosynthesis
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nocardicin A biosynthesis
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lipid A biosynthesis
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lipid IVA biosynthesis (E. coli)
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lipid IVA biosynthesis (P. putida)
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Lipopolysaccharide biosynthesis
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Purine metabolism
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purine metabolism
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acetaldehyde biosynthesis II
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long chain fatty acid ester synthesis (engineered)
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pyruvate fermentation to acetate VIII
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pyruvate fermentation to acetoin III
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beta-Alanine metabolism
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Pantothenate and CoA biosynthesis
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pantothenate biosynthesis
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phosphopantothenate biosynthesis I
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ATP biosynthesis
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Oxidative phosphorylation
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oxidative phosphorylation
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Photosynthesis
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ORGANISM
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LITERATURE
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SEQUENCE DB
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LOCALIZATION
ORGANISM
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GeneOntology No.
LITERATURE
SOURCE
additional information
in fungi, periplasmic CDAs are generally tightly coupled to a chitin synthase to rapidly deacetylate newly synthesized chitins before their maturation and crystallization. Extracellular CDAs are secreted to alter the physicochemical properties of the cell wall to either protect the cell wall from exogenous chitinases or to initiate autolysis
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Manually annotated by BRENDA team
LINKS TO OTHER DATABASES (specific for Pochonia chlamydosporia)